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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04101643
Other study ID # MRCTA, ECFAHofFMU[2019]209
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date September 29, 2019
Est. completion date January 3, 2023

Study information

Verified date November 2021
Source First Affiliated Hospital of Fujian Medical University
Contact Ying Fu
Phone 13920263588
Email fuying1995@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Spastic paraplegia type 5 (SPG5) is a rare subtype of hereditary spastic paraplegia, a highly heterogeneous group of neurodegenerative disorders defined by progressive neurodegeneration of the corticospinal tract motor neurons. SPG5 is caused by recessive mutations in the gene CYP7B1 encoding oxysterol-7a-hydroxylase. This enzyme is involved in the degradation of cholesterol into primary bile acids. CYP7B1 deficiency has been shown to lead to accumulation of neurotoxic oxysterols. Oxysterols were found to impair metabolic activity and viability of human cortical neurons at concentrations found in SPG5 patients, indicating that elevated levels of oxysterols might be key pathogenic factors in SPG5. Monoclonal antibodies that inhibit proprotein convertase subtilisin-kexin type 9 (PCSK9) have emerged as a new class of drugs that effectively lower cholesterol levels. Evolocumab, a member of this class, is a fully human monoclonal antibody that reduces LDL cholesterol levels by approximately 60%. We thus performed this interventional trial with Evolocumab 420 mg for SPG5 patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date January 3, 2023
Est. primary completion date January 3, 2023
Accepts healthy volunteers No
Gender All
Age group 14 Years to 80 Years
Eligibility Inclusion Criteria: - Age 14-80 years - Probands with clinically manifest hereditary spastic paraplegia - Genetically confirmed diagnosis of SPG5 Exclusion Criteria: - Comprised treatment with statins 3 months prior to enrolment - Contraindications to PCSK9 inhibitor therapy - Pregnancy was excluded in women of childbearing age

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
evolocumab
Eligible patients receive subcutaneous injections of evolocumab 420 mg

Locations

Country Name City State
China Department of Neurology , First Affiliated Hospital Fujian Medical University Fuzhou

Sponsors (1)

Lead Sponsor Collaborator
First Affiliated Hospital of Fujian Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The change of 27-hydroxycholesterol (27-OHC) Cholesterol is initially side chain oxidized and the resulting 27-hydroxycholesterol (27-OHC) are 7a-hydroxylated up to 4 weeks